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Brn-3 Polyclonal Antibody, 20ul Organelle Studies YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation

SKU: 26532076450

4.6
SEK111.00 SEK137.00

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Brn-3 Polyclonal Antibody, 20ul Organelle Studies YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activationPOU4F3 (POU class 4 homeobox 3) encodes a member of the POU domain family of transcription factors. POU domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in POU4F3 are the cause of non syndromic sensorineural deafness autosomal dominant type 15.

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Description

YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma) product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins

Experience clean and pure results with our 500 mL sterile vacuum filter

also called triple-A syndrome or Allgrove syndrome

suggesting additional roles for the encoded protein in the metabolism of xenobiotic compounds and the regulation of neurogenesis

nuclear protein and functions as a molecular chaperone

Brn-3 Polyclonal Antibody, 20ul Organelle Studies YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activationPOU4F3 (POU class 4 homeobox 3) encodes a member of the POU domain family of transcription factors. POU domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in POU4F3 are the cause of non syndromic sensorineural deafness autosomal dominant type 15.

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